ClinVar Miner

Submissions for variant NM_001037.5(SCN1B):c.448+278G>A

dbSNP: rs1057521627
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000892967 SCV000523854 likely benign not provided 2019-10-11 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001443075 SCV001646037 likely benign Brugada syndrome 5 2024-11-13 criteria provided, single submitter clinical testing

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